Clinical Study Coordinator - Netherlands (hybrid)

Hobson Prior are looking for a Clinical Study Coordinator to join a fantastic consultancy on a contract basis located in Leiden - Netherlands with hybrid availability. Our client is focused on supplying solutions for clients who conduct clinical trials.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• For this role, you will handle document validation and review activities.
• Responsible for resolving queries.
• Manage administrative duties such as upholding study binder, regulatory archiving, etc.
• The ideal candidate will be accountable for data entry tasks.
• Any other assigned duties.

Requirements:

• Acquaintance with eCRF.
• Familiarity with HIX (Health Manager System).
• Expertise in a study coordinator/study nurse role.
• Fluency in the English and Dutch languages.
• Obtained an IATA Certificate
• Past involvement in oncology would be ideal.
• Willing to travel to site for business needs up to 3 times a week.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.